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Clinical Dysmorphology|January 29, 2000
New clinical findings in oculo-ectodermal syndromeM Silengo, M Lerone, M Seri, et al.Clinical Dysmorphology|January 29, 2000
Craniofacial anomalies, ocular findings, pigmented nevi, camptodactyly, and skeletal changes: a possible new autosomal recessive disorderD Gül, C Oktenli, M Sağlam, et al.Clinical Dysmorphology|May 18, 1999
Siblings with a syndrome of hydrocephalus with patent aqueduct, growth retardation and associated anomaliesJ Slee, S Knowles, J GoldblattClinical Dysmorphology|May 18, 1999
Two brothers with varying combinations of severe developmental delay, epilepsy, microcephaly, tetralogy of Fallot and hydronephrosisA Ryan, J Burn, S Court, et al.Clinical Dysmorphology|May 18, 1999
A case of lateral facial clefts with Fallot tetralogy, duodenal stenosis and intestinal malrotation: a new multiple congenital anomaly syndrome?D KumarClinical Dysmorphology|May 18, 1999
New syndromic entity of situs inversus totalisM A Mubashir, M A Sabry, S Farah, et al.Clinical Dysmorphology|May 18, 1999
Further delineation of the classical Smith-Lemli-Opitz syndrome phenotype at different patient ages: clinical and biochemical studiesM Krajewska-Walasek, W Gradowska, J Ryzko, et al.Clinical Dysmorphology|May 18, 1999
Brachydactyly type B with its distinct facies and 'Cooks syndrome' are the same entityT J de Ravel, D E Berkowitz, J M Wagner, et al.Clinical Dysmorphology|May 18, 1999
Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocationT Lukusa, K Devriendt, J Jaeken, et al.Clinical Dysmorphology|May 18, 1999
Terminal transverse limb defects with tethering and omphalocele in a 17 week fetus following first trimester misoprostol exposureD R Genest, D Di Salvo, M J Rosenblatt, et al.Pageof 117